Synthesis of α-l-Threofuranosyl Nucleoside Triphosphates (tNTPs)
Organic Letters2005Vol. 7(8), pp. 1485–1487
Citations Over Time
Abstract
[structure: see text] The alpha-l-threofuranosyl nucleoside triphosphates of T, G, and D (tTTP, tGTP, and tDTP) were synthesized from the described 2'-O-DMT-protected derivatives using the Eckstein method, while the corresponding C derivative (tCTP) was prepared from the 2'-O-acetyl derivative. The prepared alpha-l-threofuranosyl nucleoside triphosphates, despite being one carbon shorter than the native 2'-deoxyfuranosyl nucleoside triphosphates, are effective substrates for selected DNA polymerases.
Related Papers
- → Nucleoside and deoxynucleoside phosphorylation in formamide solutions(1982)66 cited
- → Nucleoside Diphosphate Kinase from Microorganisms(2013)1 cited
- → Preparation of 8-Hydroxy-dGTP and 2-Hydroxy-dATP by a Phosphate Transfer Reaction by Nucleoside-Diphosphate Kinase(1999)9 cited
- → [9] The separation of nucleoside diphosphate sugars and related nucleotides by ion-exchange paper chormatography(1966)4 cited
- Nucleoside phosphorylation in amide solutions(1978)